Literature DB >> 9463463

Differential expression of Kv4 K+ channel subunits mediating subthreshold transient K+ (A-type) currents in rat brain.

P Serôdio1, B Rudy.   

Abstract

The mammalian Kv4 gene subfamily and its Drosophila Shal counterpart encode proteins that form fast inactivating K+ channels that activate and inactivate at subthreshold potentials and recover from inactivation at a faster rate than other inactivating Kv channels. Taken together, the properties of Kv4 channels compare best with those of low-voltage activating "A-currents" present in the neuronal somatodendritic compartment and widely reported across several types of central and peripheral neurons, as well as the (Ca2+-independent) transient outward potassium conductance of heart cells (Ito). Three distinct genes have been identified that encode mammalian Shal homologs (Kv4. 1, Kv4.2, and Kv4.3), of which the latter two are abundant in rat adult brain and heart tissues. The distribution in the adult rat brain of the mRNA transcripts encoding the three known Kv4 subunits was studied by in situ hybridization histochemistry. Kv4.1 signals are very faint, suggesting that Kv4.1 mRNAs are expressed at very low levels, but Kv4.2 and Kv4.3 transcripts appear to be abundant and each produces a unique pattern of expression. Although there is overlap expression of Kv4.2 and Kv4.3 transcripts in several neuronal populations, the dominant feature is one of differential, and sometimes reciprocal expression. For example, Kv4.2 transcripts are the predominant form in the caudate-putamen, pontine nucleus and several nuclei in the medula, whereas the substantia nigra pars compacta, the restrosplenial cortex, the superior colliculus, the raphe, and the amygdala express mainly Kv4.3. Some brain structures contain both Kv4.2 and Kv4.3 mRNAs but each dominates in distinct neuronal subpopulations. For example, in the olfactory bulb Kv4.2 dominates in granule cells and Kv4.3 in periglomerular cells. In the hippocampus Kv4.2 is the most abundant isoform in CA1 pyramidal cells, whereas only Kv4.3 is expressed in interneurons. Both are abundant in CA2-CA3 pyramidal cells and in granule cells of the dentate gyrus, which also express Kv4.1. In the dorsal thalamus strong Kv4.3 signals are seen in several lateral nuclei, whereas medial nuclei express Kv4.2 and Kv4.3 at moderate to low levels. In the cerebellum Kv4.3, but not Kv4.2, is expressed in Purkinje cells and molecular layer interneurons. In the cerebellar granule cell layer, the reciprocity between Kv4.2 and Kv4.3 is observed in subregions of the same neuronal population. In fact, the distribution of Kv4 channel transcripts in the cerebellum defines a new pattern of compartmentation of the cerebellar cortex and the first one involving molecules directly involved in signal processing.

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Year:  1998        PMID: 9463463     DOI: 10.1152/jn.1998.79.2.1081

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  137 in total

1.  Expression of Kv1 potassium channels in mouse hippocampal primary cultures: development and activity-dependent regulation.

Authors:  G Grosse; A Draguhn; L Höhne; R Tapp; R W Veh; G Ahnert-Hilger
Journal:  J Neurosci       Date:  2000-03-01       Impact factor: 6.167

2.  Transient potassium currents regulate the discharge patterns of dorsal cochlear nucleus pyramidal cells.

Authors:  P O Kanold; P B Manis
Journal:  J Neurosci       Date:  1999-03-15       Impact factor: 6.167

3.  Elimination of fast inactivation in Kv4 A-type potassium channels by an auxiliary subunit domain.

Authors:  Mats H Holmqvist; Jie Cao; Ricardo Hernandez-Pineda; Michael D Jacobson; Karen I Carroll; M Amy Sung; Maria Betty; Pei Ge; Kevin J Gilbride; Melissa E Brown; Mark E Jurman; Deborah Lawson; Inmaculada Silos-Santiago; Yu Xie; Manuel Covarrubias; Kenneth J Rhodes; Peter S Distefano; W Frank An
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-22       Impact factor: 11.205

4.  Evidence for the presence of a novel Kv4-mediated A-type K(+) channel-modifying factor.

Authors:  M S Nadal; Y Amarillo; E Vega-Saenz de Miera; B Rudy
Journal:  J Physiol       Date:  2001-12-15       Impact factor: 5.182

Review 5.  The other half of Hebb: K+ channels and the regulation of neuronal excitability in the hippocampus.

Authors:  Laura A Schrader; Anne E Anderson; Andrew W Varga; Michael Levy; J David Sweatt
Journal:  Mol Neurobiol       Date:  2002-02       Impact factor: 5.590

6.  Tuning pacemaker frequency of individual dopaminergic neurons by Kv4.3L and KChip3.1 transcription.

Authors:  B Liss; O Franz; S Sewing; R Bruns; H Neuhoff; J Roeper
Journal:  EMBO J       Date:  2001-10-15       Impact factor: 11.598

7.  A role for frequenin, a Ca2+-binding protein, as a regulator of Kv4 K+-currents.

Authors:  T Y Nakamura; D J Pountney; A Ozaita; S Nandi; S Ueda; B Rudy; W A Coetzee
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-16       Impact factor: 11.205

Review 8.  Active dendrites, potassium channels and synaptic plasticity.

Authors:  Daniel Johnston; Brian R Christie; Andreas Frick; Richard Gray; Dax A Hoffman; Lalania K Schexnayder; Shigeo Watanabe; Li-Lian Yuan
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2003-04-29       Impact factor: 6.237

9.  Regulation of an inactivating potassium current (IA) by the extracellular matrix protein vitronectin in embryonic mouse hippocampal neurones.

Authors:  Dmitry V Vasilyev; Michael E Barish
Journal:  J Physiol       Date:  2003-01-24       Impact factor: 5.182

10.  Voltage-dependent ion channel currents in putative neuroendocrine cells dissociated from the ventral prostate of rat.

Authors:  Jun Hee Kim; Sun Young Shin; Sang Soon Yun; Tae Jin Kim; Seung-June Oh; Kwang Myung Kim; Young-Shin Chung; Eun-Kyoung Hong; Dae-Yong Uhm; Sung Joon Kim
Journal:  Pflugers Arch       Date:  2003-02-21       Impact factor: 3.657

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